Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Fexofenadine Hydrochloride Tablets USP Recalled by Aurolife Pharma, LLC Due to Failed Impurities/Degradation Specifications
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Aurolife Pharma, LLC directly.
Affected Products
Fexofenadine Hydrochloride Tablets USP, 180 mg, packaged in a) 30-count carton (NDC 70677-0008-2) and b) 15-count carton (NDC 70677-0008-1), sunmark, Distributed by McKesson, One Post Street, San Francisco, CA 94104.
Quantity: a) 11,928 cartons; b) 288 cartons
Why Was This Recalled?
Failed Impurities/Degradation Specifications
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Aurolife Pharma, LLC
Aurolife Pharma, LLC has 14 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report